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Ackermann, S.

Publications and source records attributed to Ackermann, S..

2 recordsLinked to original sources

Unicellular propagules, cancer, and competition: Are unicellular propagules part of the optimal life-history strategy in the face of both cancer and competition?

Evolutionary transitions in individuality introduce new levels of selection and thus enable discordant selection, threatening the stability of the transition. Cheating is such a problem for multicellularity. So why have so many transitions to multicellularity persisted? One possibility is that the unicellular propagule maintains cooperation among cells by purging cheaters. The evolution of propagule size has been modeled previously, but in the absence of competition between individuals, which may often select for larger propagules. How does the nature of competition between individuals affect the optimal propagule size in the presence of cheating? Here we take a model of early multicellularity, add phenotypic switching between cheating and cooperative phenotypes, and simulate size-dependent competition on a lattice, which allows us to tune the strength of interspecific vs. intraspecific competition via dispersal. As expected, cheating favors strategies with unicellular propagules while size-dependent competition favors strategies with few large propagules (binary fragmentation). How these opposing forces resolve depends on dispersal. Local dispersal, which intensifies intraspecific competition, favors binary fragmentation, which reduces intraspecific competition for space, with one unicellular propagule. Global dispersal instead favours multiple fission when cheating is common. We also find that selfishness promotes smaller body size, despite direct opposing selection from competition. Our results shed light on the evolution of multicellular life cycles and the prevalence of a unicellular stage in the multicellular life cycle across the tree of life. Author summaryA multicellular organism is a group of cooperating cells. But wherever there is cooperation there is the temptation to cheat. Having offspring that start as a single cell (a unicellular bottleneck) has been hypothesized as an adaptation to purge lineages of cheating cells. We model the evolution of offspring size but add competition between individuals, which may select against small unicellular offspring. We find that having some unicellular offspring is still a successful strategy, but how many depends on the nature of competition.

evolutionary biology↗

Novel co-culture strategies of tumor organoids with autologous T-cells reveal clinically relevant combinations of immune-checkpoint and targeted therapies

Patient derived tumor organoids (PDTOs) have become relevant pre-clinical models for therapeutic modelling since they highly recapitulate patients response to treatment. Nevertheless, their value for immunotherapy modelling has not been fully explored. We developed a tumor processing protocol that enable the establishment of PDTOs and tumor infiltrating lymphocytes (TILs) isolation. By the optimization of functional assays, we compared the T-cells effector functions of matching PBMCs and TILs, demonstrating that PBMCs after co-culture and TILs after initial expansion display similar responses. In addition, the evaluation of cytokine production by fluorospot in combination with an image-based killing assay enable the screening of different immune-checkpoint inhibitors as well as its combination with target inhibitors. Our proof-of-concept functional assays showed the potential and versatility of PDTOs and T-cells co-culture systems for immunotherapy screening. The optimization of scalable functional assays downstream co-culture represents a significant step forward to increase the value of PDTOs as pre-clinical models for immunotherapeutic screens.

immunology↗